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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 5
2006 1
2009 5
2010 8
2011 2
2012 3
2013 2
2014 5
2015 1
2017 1
2018 2
2019 3
2020 2
2021 2
2022 2
2023 2
2024 0

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41 results

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Page 1
A patient with mosaic USP9X gene variant.
Barili V, Dall'Asta A, Uliana V, Schera GBL, Ormitti F, Romanini E, Micalizzi A, Magliozzi M, Perrino D, Novelli A, Ghi T, Percesepe A. Barili V, et al. Among authors: ormitti f. Eur J Med Genet. 2022 Dec;65(12):104638. doi: 10.1016/j.ejmg.2022.104638. Epub 2022 Oct 8. Eur J Med Genet. 2022. PMID: 36216272
High-resolution CT in diagnosis of diffuse infiltrative lung disease.
Zompatori M, Sverzellati N, Poletti V, Bnà C, Ormitti F, Spaggiari E, Maffei E. Zompatori M, et al. Among authors: ormitti f. Semin Ultrasound CT MR. 2005 Oct;26(5):332-47. doi: 10.1053/j.sult.2005.07.004. Semin Ultrasound CT MR. 2005. PMID: 16274002 Review.
Diagnostic imaging of diffuse infiltrative disease of the lung.
Zompatori M, Bnà C, Poletti V, Spaggiari E, Ormitti F, Calabrò E, Tognini G, Sverzellati N. Zompatori M, et al. Among authors: ormitti f. Respiration. 2004 Jan-Feb;71(1):4-19. doi: 10.1159/000075642. Respiration. 2004. PMID: 14872104 Free article. Review.
Bilateral cerebellopontine angle lipomas.
Ventura E, Ormitti F, Crisi G, Sanna M, Bacciu A. Ventura E, et al. Among authors: ormitti f. Auris Nasus Larynx. 2012 Feb;39(1):103-6. doi: 10.1016/j.anl.2011.01.021. Epub 2011 May 13. Auris Nasus Larynx. 2012. PMID: 21570787
Duplication of the Pituitary Gland (DPG)-Plus Syndrome Associated With Midline Anomalies and Precocious Puberty: A Case Report and Review of the Literature.
Prezioso G, Petraroli M, Bergonzani M, Davino G, Labate M, Ormitti F, Anghinoni M, Sesenna E, Esposito S. Prezioso G, et al. Among authors: ormitti f. Front Endocrinol (Lausanne). 2021 May 26;12:685888. doi: 10.3389/fendo.2021.685888. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34122353 Free PMC article. Review.
Cortical malformations and COL4A1 mutation: Three new cases.
Vitale G, Pichiecchio A, Ormitti F, Tonduti D, Asaro A, Farina L, Piccolo B, Percesepe A, Bastianello S, Orcesi S; COL4A1 International Study Group. Vitale G, et al. Among authors: ormitti f. Eur J Paediatr Neurol. 2019 May;23(3):410-417. doi: 10.1016/j.ejpn.2019.02.006. Epub 2019 Feb 22. Eur J Paediatr Neurol. 2019. PMID: 30837194
Cochlear implantation in children with cochlear nerve deficiency.
Vincenti V, Ormitti F, Ventura E, Guida M, Piccinini A, Pasanisi E. Vincenti V, et al. Among authors: ormitti f. Int J Pediatr Otorhinolaryngol. 2014 Jun;78(6):912-7. doi: 10.1016/j.ijporl.2014.03.003. Epub 2014 Mar 12. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24690223
41 results